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Clinical Study Team Assistant - UK (Remote) - FSP - Job Opportunity at Parexel

Remote, United Kingdom
Full-time
Mid-level
Posted: May 8, 2025
Remote
GBP 35,000-45,000 annually based on UK market rates for clinical research support roles

Benefits

Remote work flexibility
Professional development opportunities
Global collaboration environment
Industry-standard healthcare benefits (implied)
Company events

Key Responsibilities

Lead study-level operational support and documentation management from initialization to close-out
Maintain regulatory compliance through TMF oversight and system maintenance
Coordinate cross-functional communication and documentation across global teams
Manage budget tracking and financial oversight for clinical trials
Ensure quality control of clinical trial documentation and submissions
Facilitate Independent Oversight Committee engagement and audit preparation

Requirements

Education

Bachelor's degree with 2 years' experience, or master's degree or MBA

Experience

2+ years relevant clinical research experience

Required Skills

Proficient in Microsoft office applications (Outlook, Word, PowerPoint, Excel, TEAMS) Effective verbal and written communication skills Fluency in written and spoken English Independent work capability Multitasking and priority management Detail-oriented approach Problem solving and decision-making skills
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Sauge AI Market Intelligence

Industry Trends

Clinical trial digitalization is driving increased demand for tech-savvy clinical support professionals Decentralized clinical trials are becoming industry standard, requiring enhanced remote coordination skills Growing emphasis on data integrity and regulatory compliance is elevating the importance of clinical support roles

Role Significance

Typically works within a 10-15 person study team, coordinating with multiple functional areas
Mid-level position with significant operational responsibility and indirect influence on clinical trial success

Key Projects

Clinical trial documentation management and quality control Regulatory compliance and audit preparation Cross-functional team coordination and communication Budget tracking and financial oversight

Success Factors

Strong attention to detail and organizational skills Ability to work independently while maintaining effective team communication Understanding of clinical research processes and regulatory requirements Proactive problem-solving approach

Market Demand

High demand due to increasing clinical trial complexity and regulatory requirements

Important Skills

Critical Skills

Clinical research process knowledge Regulatory compliance understanding Documentation management expertise Cross-functional communication skills

Beneficial Skills

Project management capabilities Financial tracking experience Quality management systems knowledge Clinical data management familiarity

Unique Aspects

Fully remote position offering exceptional work-life balance
Global exposure through international project teams
Comprehensive involvement in clinical trial lifecycle

Career Growth

2-3 years in role before advancement, depending on performance and project exposure

Potential Next Roles

Clinical Research Associate Clinical Project Manager Clinical Operations Manager Study Start-up Specialist

Company Overview

Parexel

Parexel is a leading global clinical research organization (CRO) providing comprehensive clinical development and commercialization services

Top-tier CRO with strong market presence and established reputation in clinical research industry
Significant UK presence with robust remote work infrastructure
Professional environment with emphasis on quality, compliance, and global collaboration
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  • Salary estimates and market demand analysis
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  • Critical success factors and key skills
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